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Ractopamine hydrochloride

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Identification
Molecular formula
C18H23NO3·HCl
CAS number
90274-24-1
IUPAC name
4-[2-[[2-(1,3-benzodioxol-5-yl)-1-methyl-ethyl]amino]-1-hydroxy-ethyl]benzene-1,2-diol;hydrochloride
State
State

At room temperature, Ractopamine hydrochloride is in a solid state, appearing as a powder.

Melting point (Celsius)
244.00
Melting point (Kelvin)
517.00
Boiling point (Celsius)
258.50
Boiling point (Kelvin)
531.70
General information
Molecular weight
337.83g/mol
Molar mass
337.8180g/mol
Density
1.2130g/cm3
Appearence

Ractopamine hydrochloride is a white to off-white crystalline powder. It is typically odorless and is readily soluble in acidic conditions.

Comment on solubility

Solubility of 4-[2-[[2-(1,3-benzodioxol-5-yl)-1-methyl-ethyl]amino]-1-hydroxy-ethyl]benzene-1,2-diol; hydrochloride

The solubility of 4-[2-[[2-(1,3-benzodioxol-5-yl)-1-methyl-ethyl]amino]-1-hydroxy-ethyl]benzene-1,2-diol; hydrochloride can be characterized as follows:

  • Hydrochloride Form: The presence of a hydrochloride group generally enhances the solubility of the compound in aqueous environments.
  • Polar Character: The structure contains multiple hydroxyl (-OH) groups, which contributes to its polarity, making it more soluble in water.
  • Organic Solvents: Due to the presence of hydrophobic aromatic rings, this compound may exhibit variable solubility in organic solvents such as ethanol or methanol.
  • Temperature Effect: As with many compounds, solubility can be sensitive to temperature changes; typically, an increase in temperature may enhance solubility.

In summary, while the hydrochloride salt form aids in solubility, the complete behavior of this compound in various solvents will depend on specific conditions, including pH and temperature. This multifaceted solubility profile makes it particularly interesting for both laboratory and pharmaceutical applications.

Interesting facts

Interesting Facts about 4-[2-[[2-(1,3-benzodioxol-5-yl)-1-methyl-ethyl]amino]-1-hydroxy-ethyl]benzene-1,2-diol; hydrochloride

This compound, commonly recognized in scientific literature, possesses a unique molecular structure and intriguing applications. Here are some fascinating points about it:

  • Pharmacological Potential: The compound belongs to a class of compounds with recognized therapeutic activities. It has been studied for its potential use in the treatment of various conditions, including cardiovascular issues and cognitive disorders.
  • Complex Structure: Its structural composition involves multiple functional groups that enhance its biological activity. The presence of the benzodioxole moiety suggests that it may interact with neurotransmitter systems.
  • Research Insights: According to recent studies, this compound's ability to modulate specific pathways could lead to promising results in drug development. Researchers have highlighted its role as a lead compound in synthesizing novel therapeutic agents.
  • Synergy with Other Compounds: The hydrochloride form indicates enhanced solubility and bioavailability, essential for pharmacological efficacy. This aspect allows for potential combination therapies where synergistic effects can be maximized.
  • Environmental Relevance: Beyond its medicinal properties, compounds similar to this one are often evaluated for their environmental impact, especially if they are used in pharmaceuticals. Monitoring their ecological footprint is crucial.

In summary, 4-[2-[[2-(1,3-benzodioxol-5-yl)-1-methyl-ethyl]amino]-1-hydroxy-ethyl]benzene-1,2-diol; hydrochloride is more than just a chemical entity. It embodies a multifaceted potential waiting to be explored further in both medicinal chemistry and environmental studies. As scientists delve deeper into its properties, we can expect to uncover even more insights into its applications and benefits.

Synonyms
Protokylol hydrochloride
Palison
136-69-6
Protokylol HCl
Asmetil
Biturix
Beres
Caytine hydrochloride
Atma-sanol
EINECS 205-254-8
UNII-7U7O8Q48IO
NSC 113490
NSC-113490
7U7O8Q48IO
Protokylol (hydrochloride)
Caytine hydrochloride; NSC 113490
1,2-Benzenediol, 4-(2-((2-(1,3-benzodioxol-5-yl)-1-methylethyl)amino)-1-hydroxyethyl)-, HCl
4-(2-((2-(1,3-Benzodioxol-5-yl)-1-methylethyl)amino)-1-hydroxyethyl)-1,2-benzenediol HCl
4-[2-[1-(1,3-benzodioxol-5-yl)propan-2-ylamino]-1-hydroxyethyl]benzene-1,2-diol;hydrochloride
1,2-Benzenediol, 4-(2-((2-(1,3-benzodioxol-5-yl)-1-methylethyl)amino)-1-hydroxyethyl)-, hydrochloride
alpha-(((alpha-Methyl-3,4-methylenedioxyphenethyl)amino)methyl)protocatechuyl alcohol, hydrochloride
Benzyl alcohol, 3,4-dihydroxy-alpha-(((alpha-methyl-3,4-(methylenedioxy)phenethyl)amino)methyl)-, hydrochloride
PROTOKYLOL HYDROCHLORIDE (MART.)
PROTOKYLOL HYDROCHLORIDE [MART.]
Protokylol Hydrochloride(Mixture of Diastereomers)
Protokylolhydrochlorid
Protoklol hydrochloride
4-(2-{[2-(1,3-benzodioxol-5-yl)-1-methylethyl]amino}-1-hydroxyethyl)-1,2-benzenediol hydrochloride
SCHEMBL210099
CHEMBL1200893
DTXSID30929210
LOVXREQUMZKFCM-UHFFFAOYSA-N
NSC113490
PROTOKYLOL HYDROCHLORIDE [MI]
PROTOKYLOL HYDROCHLORIDE [WHO-DD]
AS-85626
HY-16413
CS-0006327
NS00079652
PROTOKYLOL HYDROCHLORIDE [GREEN BOOK]
PROTOKYLOL HYDROCHLORIDE [ORANGE BOOK]
G91339
Q27268861
WLN: T56 BO DO CHJ G1Y1 & M1YQR CQ DQ & GH
1, 4-[2-[[2-(1,3-benzodioxol-5-yl)-1-methylethyl]amino]-1-hydroxyethyl]-, hydrochloride
.ALPHA.-(((.ALPHA.-METHYL-3,4-METHYLENEDIOXYPHENETHYL)AMINO)METHYL)PROTOCATECHUYL ALCOHOL, HYDROCHLORIDE
205-254-8
4-(2-{[1-(2H-1,3-Benzodioxol-5-yl)propan-2-yl]amino}-1-hydroxyethyl)benzene-1,2-diol--hydrogen chloride (1/1)
Benzyl alcohol,4-dihydroxy-.alpha.-[[[.alpha.-methyl-3,4-(methylenedioxy)phenethyl]amino]methyl]-, hydrochloride